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author:

Wang, Z.-W. (Wang, Z.-W..) [1] | Su, D. (Su, D..) [2] | Li, X.-Q. (Li, X.-Q..) [3] | Cao, J.-J. (Cao, J.-J..) [4] | Yang, D.-C. (Yang, D.-C..) [5] | Liu, J.-Y. (Liu, J.-Y..) [6]

Indexed by:

Scopus

Abstract:

In this study, we demonstrate a novel H2O2 activatable photosensitizer (compound 7) which contains a diiodo distyryl boron dipyrromethene (BODIPY) core and an arylboronate group that quenches the excited state of the BODIPY dye by photoinduced electron transfer (PET). The BODIPY-based photosensitizer is highly soluble and remains nonaggregated in dimethyl sulfoxide (DMSO) as shown by the intense and sharp Q-band absorption (707 nm). As expected, compound 7 exhibits negligible fluorescence emission and singlet oxygen generation efficiency. However, upon interaction with H2O2, both the fluorescence emission and singlet oxygen production of the photosensitizer can be restored in phosphate buffered saline (PBS) solution and PBS buffer solution containing 20% DMSO as a result of the cleavage of the arylboronate group. Due to the higher concentration of H2O2 in cancer cells, compound 7 even with low concentration is particularly sensitive to human cervical carcinoma (HeLa) cells (IC50 = 0.95 μM) but hardly damage human embryonic lung fibroblast (HELF) cells. The results above suggest that this novel BODIPY derivative is a promising candidate for fluorescence imaging-guided photodynamic cancer therapy. © 2018 by the authors.

Keyword:

Activatable photosensitizers; H2O2-responsive; Photodynamic therapy; Photoinduced electron transfer (PET)

Community:

  • [ 1 ] [Wang, Z.-W.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [Su, D.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 3 ] [Li, X.-Q.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 4 ] [Cao, J.-J.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 5 ] [Yang, D.-C.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 6 ] [Liu, J.-Y.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou University, Fuzhou, 350108, China

Reprint 's Address:

  • [Liu, J.-Y.]State Key Laboratory of Photocatalysis on Energy and Environment, National and Local Joint Biomedical Engineering Research Center on Photodynamic Technologies, College of Chemistry, Fuzhou UniversityChina

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Source :

Molecules

ISSN: 1420-3049

Year: 2019

Issue: 1

Volume: 24

Page: 1-15

3 . 2 6 7

JCR@2019

4 . 2 0 0

JCR@2023

ESI HC Threshold:184

CAS Journal Grade:3

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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